← Back to catalogue

RFP-100A Connector Cable

FDA UDI

Class II (US FDA UDI)

by Baylis Medical Technologies Inc

Identity

Trade Name
RFP-100A Connector Cable FDA UDI
Generic Name
Electrical-only medical device connection cable, single-use FDA UDI
Model / Reference
RFX-BAY-OTW-10-SU FDA UDI

Identifiers

Primary DI / UDI-DI
07540299000167 FDA UDI
510(k) Number
K230571 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrical-only medical device connection cable, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 10 Feet FDA UDI

Category: Electrical-only medical device connection cable, single-use

RFP-100A Connector Cable by Baylis Medical Technologies Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b2d7278e-f991-4cf2-b978-cbde7bb79daa 35 fields · synced May 30, 2026